Goose Creek Hand Sanitizer Recalled for Chemical Contamination
Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer Aloe Watermelon Lemonade due to contamination with methanol, benzene, and acetaldehyde. The 3.38 FL. OZ. bottles were distributed nationwide.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Our severity reasoning: This recall is classified as FDA Class I by the issuing agency. Per the severity rubric, FDA Class I recalls are classified as Critical (score 5), as they involve products that may cause serious adverse health consequences or death.
Plain-English summary
Scentsational Soaps & Candles Inc is recalling Goose Creek Hand Sanitizer Aloe Watermelon Lemonade, 3.38 FL. OZ. (100 mL) spray bottles, UPC 814630 02423 3, Lot #20259. The product was found to be contaminated with methanol (wood alcohol), benzene, and acetaldehyde.
This product was distributed nationwide in the United States. Consumers who have purchased this hand sanitizer should stop using it immediately and dispose of the product safely.
For questions or to report any adverse effects from using this product, consumers should contact the FDA or the recalling manufacturer, Scentsational Soaps & Candles Inc, located at 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539.
The recalled product
- Product
- Goose Creek Hand Sanitizer aloe Watermelon Lemonade, Anti-Bacterial Spray, 3.38 FL. OZ. (100 mL), Goose Creek www.GooseCreekCandle.com, 1498 S. Wallace Wilkinson Blvd., Liberty, KY 42539, UPC 814630 02423 3
- Manufacturer
- Scentsational Soaps & Candles Inc
- Category
- Drug — Hand Sanitizer
- Hazard
- methanol
- benzene
- acetaldehyde
- chemical-contamination
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot #: 20259
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- SevereErythromycin Tablets Recalled for Impurity Above Acceptable Limits
FDA (Drugs) · 2026-05-27
- SevereAtomoxetine Capsules Recalled Due to Labeling Mix-Up Error
FDA (Drugs) · 2026-05-27
- ModeratePrimidone Tablets Recalled Due to API Cross-Contamination
FDA (Drugs) · 2026-05-27
- SevereCIMZIA injection recalled due to lack of sterility assurance
FDA (Drugs) · 2026-05-27